Epilepsy due to X-linked recessive progressive myoclonic epilepsy with ataxia (Q86435): Difference between revisions

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Latest revision as of 11:50, 15 August 2026

Epilepsy due to a wide variety of clinical conditions having in common an X-linked genetic defect. Phenotype varies with the age of the patient. Seizure semiology and electroencephalographic features are indistinguishable. Excludes genetic syndromes primarily expressed as epilepsy.

Language	Label	Description	Also known as
default for all languages	ID_1252358703
English	Epilepsy due to X-linked recessive progressive myoclonic epilepsy with ataxia	Epilepsy due to a wide variety of clinical conditions having in common an X-linked genetic defect. Phenotype varies with the age of the patient. Seizure semiology and electroencephalographic features are indistinguishable. Excludes genetic syndromes primarily expressed as epilepsy.